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| Job #02610 |
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| About our client |
| Our client is a reputable, mid-size CRO that is experiencing unprecedented growth. The company has an experienced management team, a varied selection of interesting protocols and an empowering corporate culture that is focused on the long-term professional development of its employees. |
| Position |
Location |
| Clinical Project Manager (Home-Based) |
USA |
| Salary |
Reports to |
| Highly competitive package, commensurate with experience | Management |
| Responsibilities |
1) Provide project-specific support as the primary contact for project coordinators, CRAs, internal key clinical personnel and investigational site personnel 2) Train CRAs in project-specific areas and administering conduct of trials 3) Perform all tasks done by CRAs (if required) 4) Track the status of projects with support from logistics coordinators 5) Monitor on-site study progress and contribute to the writing of study summary reports for agency/sponsor submission 6) Track reporting and follow up on serious adverse events with support from logistics coordinators |
| Requirements |
1) Bachelor's degree in a scientific discipline 2) 4+ years of clinical trial experience in the pharmaceutical or biotech industry, including both site management and project management 3) 3+ years of field monitoring experience 4) Strong knowledge and understanding of FDA regulations and GCPs 5) Knowledge of current federal regulations and guidelines 6) Highly effective in setting/meeting personal short/long term goals to complete assignments 7) Ability to anticipate problems relating to projects and develop/implement solutions 8) Solid leadership skills 9) Highly developed interpersonal and communication (written/oral) skills 10) Willingness to travel – up to 20% |

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